Výsledky vyhledávání - "Min-Wei Gong"

A C1976Y missense mutation in the mouse Ip3r1 gene leads to short-term mydriasis and unfolded protein response in the iris constrictor muscles

Autor: Yi Wang, Min-Wei Gong, Shun Yang, Meng-Jun Dai, Zheng-Feng Xue, Hong-Ling Wang, Rui Chen, Ya-You Miao, Xiao-Ge Duan, Li Chen, Bing Chen, Chong-Yang Qi, Wan-E Wei

Publikováno v: Experimental Animals

Ip3r1 encodes an inositol 1,4,5-trisphosphate-responsive calcium channel. Mutations in the IP3R1 gene in humans may cause Gillespie syndrome (GS) typically presents as fixed dilated pupils in affected infants, which was referred to as iris hypoplasia

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f97d41ff7e067fcf6ef0e4224ce4f2c8
http://europepmc.org/articles/PMC7004804

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A missense mutation of Ip3r1 in Dp2 mice leads to short-term mydriasis and unfolded protein response in the iris constrictor muscles

Autor: Shun Yang, Zhengfeng Xue, Li Chen, Chong-Yang Qi, Bing Chen, Hong-Ling Wang, Wan-E Wei, Rui Chen, Min-Wei Gong, Meng-Jun Dai, Xiao-Ge Duan, Yi Wang, Ya-You Miao

Ip3r1 encodes an inositol 1,4,5-triphosphate-responsive calcium channel. Mutations in the Ip3r1 gene in humans may cause Gillespie syndrome (GS) typically presents as fixed dilated pupils in affected infants, which was referred to as iris hypoplasia.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::902d58ce997124e6e26d7297972c730c
https://doi.org/10.1101/465591

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